FDA Recall United States Terminated Historical recordClass III
Swire Coca Cola USA
- Product
- Caffeine-Free Barq s Root Beer 12 Pack, 12 oz cans
- Published
- October 3, 2018
- Distribution
- Nationwide
Swire Coca Cola USA Recall: Exterior packaging correctly identifies the contents as Cherry Coca-Cola Zero, the cans contained in the fridge pack are incorrectly labeled as Cherry Coca-Cola and do not include the required notification for phenylketonurics that the beverage contains phenylalanine.
United States
TerminatedClass II
- Company
- Swire Coca Cola USA
- Product
- Coca-Cola Cherry Zero Sugar Fridge Pack, 12 - 12 FL OZ CANS…
- Recall date
- February 19, 2022
- Terminated
- April 27, 2022
- Source
- FDA
Reason for recall
Exterior packaging correctly identifies the contents as Cherry Coca-Cola Zero, the cans contained in the fridge pack are incorrectly labeled as Cherry Coca-Cola and do not include the required notification for phenylketonurics that the beverage contains phenylalanine.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Coca-Cola Cherry Zero Sugar Fridge Pack, 12 - 12 FL OZ CANS (144 FL OZ) in a 12-pack fridge pack carton. UPC 049000047516; UPC Cherry Coca-Cola Zero Sugar can 049000047561; Cherry Coca-Cola can 04905004. There are 2 12-packs per case. | 049000047516 | 740 cases (2 12-packs/case) | Cherry Coca-Cola Zero Sugar, MAY3022TOA 15:25 -16:15 (time stamps) 12 oz. can in a 12-pack fridge pack. Cherry Coca-Cola, MAY3022TOA, 12 oz. can (Single Cans Only) *If removed from the above 12 pack at the store for individual sale. |
Distribution
- AZ
- UT
- WY
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0854-2022
- Event ID
- 89654
- Status
- Terminated
- Classification
- Class II
- Company
- Swire Coca Cola USA
- Product description
- Coca-Cola Cherry Zero Sugar Fridge Pack, 12 - 12 FL OZ CANS (144 FL OZ) in a 12-pack fridge pack carton. UPC 049000047516; UPC Cherry Coca-Cola Zero Sugar can 049000047561; Cherry Coca-Cola can 04905004. There are 2 12-packs per case.
- Quantity
- 740 cases (2 12-packs/case)
- Reason
- Exterior packaging correctly identifies the contents as Cherry Coca-Cola Zero, the cans contained in the fridge pack are incorrectly labeled as Cherry Coca-Cola and do not include the required notification for phenylketonurics that the beverage contains phenylalanine.
- Recall initiation date
- February 19, 2022
- Report date
- March 16, 2022
- Classification date
- Not published in this source record
- Termination date
- April 27, 2022
- Distribution pattern
- AZ, UT, WY
- UPC, lot, and code information
- UPC 049000047516; Cherry Coca-Cola Zero Sugar, MAY3022TOA 15:25 -16:15 (time stamps) 12 oz. can in a 12-pack fridge pack. Cherry Coca-Cola, MAY3022TOA, 12 oz. can (Single Cans Only) *If removed from the above 12 pack at the store for individual sale.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Swire Coca Cola USA
Other recalls from Swire Coca Cola USA
FDA Recall United States Terminated Historical recordClass II
Swire Coca Cola USA
- Product
- Dr. Pepper Est. 1885 Diet, 20 FL Oz (1.25 PT), 591 mL
- Published
- April 25, 2018
- Distribution
- Nationwide
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Arizona | 1 |
| Utah | 1 |
| Wyoming | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
